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Published on: January 27, 2019
Probiotics and the development of very low birthweight infants: follow-up study of a randomised trial
Satsuki Totsu, Masaki Terahara1, Satoshi Kusuda2
1Food Science Research Laboratories, Meiji Co., Ltd., Odawara, Japan.
Insights
Bifidobacterium bifidum OLB6378 supplementation may improve neurodevelopment in very low birthweight infants. This probiotic intervention showed a more favorable developmental quotient distribution at 18 months corrected age compared to placebo.
Area of Science:
- Neonatal Medicine
- Microbiology
- Developmental Pediatrics
Background:
- Very low birthweight (VLBW) infants face developmental challenges.
- Early life gut microbiota influences neurodevelopment.
- Bifidobacterium bifidum strains are explored for their health benefits.
Purpose of the Study:
- To evaluate the impact of Bifidobacterium bifidum OLB6378 on the neurodevelopment of VLBW infants.
- To assess developmental outcomes at 18 months corrected age.
Main Methods:
- A long-term follow-up of a cluster-randomised, placebo-controlled trial.
- VLBW infants received either Bifidobacterium bifidum OLB6378 or placebo from birth.
- Developmental quotient (DQ18) was assessed at 18 months corrected age.
Main Results:
- The Bifidobacterium bifidum OLB6378 group showed a significantly more favorable distribution of DQ18 scores compared to the placebo group.
- Specifically, higher proportions of infants in the OLB6378 group achieved average or better development (≥100).
- Statistical analysis indicated a significant positive effect (P=0.038).
Conclusions:
- Bifidobacterium bifidum OLB6378 supplementation shows potential benefits for the psychological development of VLBW infants.
- Further studies are warranted, considering the assessment rates.
- Probiotic interventions may be a promising strategy for supporting VLBW infant neurodevelopment.
Objective:
To investigate the effect of Bifidobacterium bifidum OLB6378 on the development of very low birthweight (VLBW) infants at 18 months of corrected age.
Design:
Long-term follow-up study of a cluster-randomised, placebo-controlled trial.
Patients:
VLBW infants (birth weight <1500 g) born between January 2010 and March 2011 and managed at 19 neonatal intensive care unit facilities assigned to two groups to account for the effect of probiotic cross-contamination within facilities.
Interventions:
For VLBW infants, administration of OLB6378 as a probiotic was started within 48 hours of birth and continued until the body weight reached 2000 g.
Main Outcome Measures:
At 18 months of corrected age, physical status and developmental quotient (DQ18) were assessed. The distribution of DQ18 scores was categorised into four levels of development: <70, significant developmental delay; 70-84, moderate developmental delay; 85-99, without developmental delay; ≥100, average development or better.
Results:
Among 153 infants assigned to the OLB6378 administration group and 130 assigned to the placebo administration group, 102 and 105 infants, respectively, underwent the 18-month medical examination. The distribution of developmental levels (DQ18 scores <70, 70-84, 85-99 and ≥100) was significantly more favourable for OLB6378 administration (12, 12, 25 and 40 infants, respectively) than for placebo administration (15, 17, 23 and 24 infants, respectively) (ordered logistic regression analysis: partial correlation coefficient, 0.589; P value, 0.038).
Conclusions:
Although limited by assessment rates, result suggests that OLB6378 may have a beneficial effect on the psychological development in VLBW infants.
Clinical Trial Registration:
UMIN000002543.
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